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Site Research Assistant - Kenosha, Wi

1 year years
$25.00 – $39.00
10 Aug. 29, 2025
Job Description
Job Type: Part Time Education: High School Diploma plus 1 year of relevant clinical research experience. Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title: Site Research Assistant

Location: Kenosha, Wisconsin
Job Type: Part-Time
Work Set-Up: On-Site (Office-Based)
Weekly Hours: 24 hours/week
Job ID: R1495515
Company: IQVIA
Availability: Position also open in additional locations


Position Summary:

This role supports clinical trial activities by working closely with site teams and investigators to ensure trials are conducted in compliance with regulatory standards. The ideal candidate demonstrates strong interpersonal skills, logical thinking, adaptability, and an ability to prioritize effectively in a fast-paced environment.


Key Responsibilities:

Clinical Trial Support

  • Assist with EDC entry and resolution of queries.

  • Develop and maintain effective communication with study team members.

  • Build trusting relationships with investigators and clinic staff.

Participant Management

  • Screen, recruit, and enroll research subjects.

  • Schedule subject visits and procedures.

  • Collect patient/research participant history.

  • Coordinate follow-up care and laboratory procedures.

  • Assist in the informed consent process.

  • Support participant safety throughout study participation.

Compliance and Documentation

  • Ensure adherence to IRB-approved protocols.

  • Comply with IQVIA, sponsor SOPs, policies, and relevant regulations.

  • Coordinate protocol-related procedures and document accordingly.


Qualifications:

Minimum Requirements:

  • High School Diploma plus 1 year of relevant clinical research experience.

  • Ability to manage clinical responsibilities and meet timelines with minimal supervision.

Preferred:

  • At least 1 year of experience in a clinical research setting.

  • Working knowledge of clinical trial processes, Good Clinical Practices (GCP), and medical terminology.

  • Understanding of protocol-specific procedures, study schedules, and consent forms.

  • Clinical skills in collecting data and performing routine procedures.

Skills:

  • Attention to detail and high level of accuracy.

  • Strong communication and team collaboration skills.

  • Proficiency in building effective working relationships with coworkers, physicians, patients, and sponsors.

  • Ability to manage multiple priorities and adapt quickly to changes.

Licensing & Certification:

  • Must hold any applicable certifications/licenses required by local/state/national regulatory bodies or company policies.

🔒 Please note: This position is not eligible for employer-sponsored work visa support.


Compensation:

  • Hourly Pay Range: $25.00 – $39.00
    (Actual rate may vary depending on experience, qualifications, schedule, and location.)

  • May include bonuses, incentives, and a comprehensive benefits package.


About IQVIA:

IQVIA is a global leader in clinical research, healthcare intelligence, and real-world data. We empower life sciences companies with technology and insights to advance medical innovation and improve patient outcomes worldwide.
🔗 Learn more: https://jobs.iqvia.com


Equal Opportunity Employer:

IQVIA is an Equal Opportunity Employer. All qualified applicants will receive consideration regardless of race, religion, gender identity, sexual orientation, disability, veteran status, or other protected categories.
🔗 EEO Policy: https://jobs.iqvia.com/eoe


How to Apply:

Visit https://jobs.iqvia.com and search for Job ID: R1495515, or click Apply Now on the job posting.